Allele Registry

Canonical Allele Identifier: PA105016

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011047

ClinVar Variation:

10334

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg2323His	CA255226 NM_000132.4:c.6968G>A